利用遗传标记线粒体DNA细胞色素b分析北Bengkulu地区Ketahun加工牛肉肉丸中猪肉含量

Sipriyadi, Hasriany Vellarenza, C. Muslim
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引用次数: 0

摘要

本研究旨在分析北Bengkulu地区出售的肉丸中猪肉的含量。该研究于2019年12月至2020年5月进行。肉丸样本取自北Bengkulu区Ketahun的12个肉丸商人摊位。使用dnasy指南和协议®mericon®Food Qiagen Mini Kit从肉丸中分离DNA基因组样本。采用正向通用引物、反向奶牛引物、反向猪引物、反向混合引物PCR (Polymerase Chain Reaction,聚合酶链式反应)等方法扩增线粒体DNA Cyt b基因,共30个循环。扩增结果用1%琼脂糖凝胶电泳,用紫外透光凝胶文件系统(UV Transluminator gel Document System)进行可视化。然后对获得的数据进行分析。每个样品的DNA条带在凝胶琼脂糖上可视化,与标记1kb,大小为398 bp(猪含量标记)相比。调查结果显示,12个肉丸样品中有5个被猪肉污染,分别是BU7、BU8、BU9、BU11和BU12。肉丸上的猪肉含量信息可以作为明古鲁省食品安全政策的决定材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Analysis of Pork Content in Processed Beef Meatballs at Ketahun, North Bengkulu District Using Genetic Marker Mitochondrial DNA Cytochrome b
This research aims to analyze the content of pork in the sold meatballs in the North Bengkulu district. The study was conducted in December 2019-May 2020. Meatball samples were taken from 12 meatball merchant stalls in Ketahun, North Bengkulu district. DNA genome samples were isolated from the meatball using DNeasy guidelines and protocols® mericon® Food Qiagen Mini Kit. The Cyt b gene of mitochondrial DNA was amplified using forward universal primer, reverse cow primer, reverse pig primer, and reverse mixed primer PCR (Polymerase Chain Reaction) as much as 30 cycles. The amplification result was running on electrophoresis with agarose gel 1% and visualized with UV Transluminator Gel Document System Axygen. The data obtained were then analyzed. The DNA band of each sample was visualized on gel agarose compared to marker 1 Kb with a size of 398 bp (pig content marker). The results of the study showed that there were five of twelve meatball samples were contaminated with pork, namely BU7, BU8, BU9, BU11, and BU12. The information of pork content on meatballs can be used as a determining material in food safety policy in Bengkulu Province.
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